File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Spectroscopic study of the dehydration and/or dehydroxylation of phyllosilicate and zeolite minerals

TitleSpectroscopic study of the dehydration and/or dehydroxylation of phyllosilicate and zeolite minerals
Authors
Issue Date2011
Citation
Journal of Geophysical Research E: Planets, 2011, v. 116, n. 5 How to Cite?
AbstractPhyllosilicates on Mars mapped by infrared spectroscopic techniques could have been affected by dehydration and/or dehydroxylation associated with chemical weathering in hyperarid conditions, volcanism or shock heating associated with meteor impact. The effects of heat-induced dehydration and/or dehydroxylation on the infrared spectra of 14 phyllosilicates from four structural groups (kaolinite, smectite, sepiolite-palygorskite, and chlorite) and two natural zeolites are reported here. Pressed powders of size-separated phyllosilicate and natural zeolite samples were heated incrementally from 100°C to 900°C, cooled to room temperature, and measured using multiple spectroscopic techniques: midinfrared (400-4000 cm -1) attenuated total reflectance, midinfrared reflectance (400-1400 cm -1), and far-infrared reflectance (50-600 cm -1) spectroscopies. Correlated thermogravimetric analysis and X-ray diffraction data were also acquired in order to clarify the thermal transformation of each sample. For phyllosilicate samples, the OH stretching (∼3600 cm -1), OH bending (∼590-950 cm -1), and/or H 2O bending (∼1630 cm -1) bands all become very weak or completely disappear upon heating to temperatures > 500°C. The spectral changes associated with SiO 4 vibrations (∼1000 cm -1 and ∼500 cm -1) show large variations depending on the compositions and structures of phyllosilicates. The thermal behavior of phyllosilicate IR spectra is also affected by the type of octahedral cations. For example, spectral features of Al 3+-rich smectites are more stable than those of Fe 3+-rich smectites. The high-temperature (>800°C) spectral changes of trioctahedral Mg 2+-rich phyllosilicates such as hectorite, saponite, and sepiolite result primarily from crystallization of enstatite. Phyllosilicates with moderate Mg 2+ concentration (e.g., palygorskite, clinochlore) and dioctahedral montmorillonites (e.g., SAz-1 and SCa-3) with partial Mg 2+-for- Al 3+ substitution all have new spectral feature developed at ∼900 cm -1 upon heating to 800C. Compared with phyllosilicates, spectral features of two natural zeolites, clinoptilolite and mordenite, are less affected by thermal treatments. Even after heating to 900C, the IR spectral features attributed to Si (Al)-O stretching and bending vibration modes do not show significant differences from those of unheated zeolites. Copyright 2011 by the American Geophysical Union.
Persistent Identifierhttp://hdl.handle.net/10722/236655
ISSN
2015 Impact Factor: 3.318
2020 SCImago Journal Rankings: 1.670
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChe, Congcong-
dc.contributor.authorGlotch, Timothy D.-
dc.contributor.authorBish, David L.-
dc.contributor.authorMichalski, Joseph R.-
dc.contributor.authorXu, Wenqian-
dc.date.accessioned2016-12-01T09:08:31Z-
dc.date.available2016-12-01T09:08:31Z-
dc.date.issued2011-
dc.identifier.citationJournal of Geophysical Research E: Planets, 2011, v. 116, n. 5-
dc.identifier.issn0148-0227-
dc.identifier.urihttp://hdl.handle.net/10722/236655-
dc.description.abstractPhyllosilicates on Mars mapped by infrared spectroscopic techniques could have been affected by dehydration and/or dehydroxylation associated with chemical weathering in hyperarid conditions, volcanism or shock heating associated with meteor impact. The effects of heat-induced dehydration and/or dehydroxylation on the infrared spectra of 14 phyllosilicates from four structural groups (kaolinite, smectite, sepiolite-palygorskite, and chlorite) and two natural zeolites are reported here. Pressed powders of size-separated phyllosilicate and natural zeolite samples were heated incrementally from 100°C to 900°C, cooled to room temperature, and measured using multiple spectroscopic techniques: midinfrared (400-4000 cm -1) attenuated total reflectance, midinfrared reflectance (400-1400 cm -1), and far-infrared reflectance (50-600 cm -1) spectroscopies. Correlated thermogravimetric analysis and X-ray diffraction data were also acquired in order to clarify the thermal transformation of each sample. For phyllosilicate samples, the OH stretching (∼3600 cm -1), OH bending (∼590-950 cm -1), and/or H 2O bending (∼1630 cm -1) bands all become very weak or completely disappear upon heating to temperatures > 500°C. The spectral changes associated with SiO 4 vibrations (∼1000 cm -1 and ∼500 cm -1) show large variations depending on the compositions and structures of phyllosilicates. The thermal behavior of phyllosilicate IR spectra is also affected by the type of octahedral cations. For example, spectral features of Al 3+-rich smectites are more stable than those of Fe 3+-rich smectites. The high-temperature (>800°C) spectral changes of trioctahedral Mg 2+-rich phyllosilicates such as hectorite, saponite, and sepiolite result primarily from crystallization of enstatite. Phyllosilicates with moderate Mg 2+ concentration (e.g., palygorskite, clinochlore) and dioctahedral montmorillonites (e.g., SAz-1 and SCa-3) with partial Mg 2+-for- Al 3+ substitution all have new spectral feature developed at ∼900 cm -1 upon heating to 800C. Compared with phyllosilicates, spectral features of two natural zeolites, clinoptilolite and mordenite, are less affected by thermal treatments. Even after heating to 900C, the IR spectral features attributed to Si (Al)-O stretching and bending vibration modes do not show significant differences from those of unheated zeolites. Copyright 2011 by the American Geophysical Union.-
dc.languageeng-
dc.relation.ispartofJournal of Geophysical Research E: Planets-
dc.titleSpectroscopic study of the dehydration and/or dehydroxylation of phyllosilicate and zeolite minerals-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1029/2010JE003740-
dc.identifier.scopuseid_2-s2.0-79958052135-
dc.identifier.volume116-
dc.identifier.issue5-
dc.identifier.spagenull-
dc.identifier.epagenull-
dc.identifier.isiWOS:000291103300001-
dc.identifier.issnl0148-0227-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats